Molecular Psychiatry, 1359-4184

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  1. 2017
  2. 2016
  3. CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders

    Råstam, M. & 35 others Mercati, O., Huguet, G., Danckaert, A., André-Leroux, G., Maruani, A., Bellinzoni, M., Rolland, T., Gouder, L., Mathieu, A., Buratti, J., Amsellem, F., Benabou, M., Van-Gils, J., Beggiato, A., Konyukh, M., Bourgeois, J-P., Gazzellone, M. J., Yuen, R. K. C., Walker, S., Delépine, M., Boland, A., Régnault, B., Francois, M., Van Den Abbeele, T., Mosca-Boidron, A. L., Faivre, L., Shimoda, Y., Watanabe, K., Bonneau, D., Leboyer, M., Scherer, S. W., Gillberg, C., Delorme, R., Cloëz-Tayarani, I. & Bourgeron, T. 2016 May 10 In : Molecular Psychiatry. 9 p.

    Research output: Contribution to journalArticle

  4. Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism

    Råstam, M. & 26 others Pilorge, M., Fassier, C., Le Corronc, H., Potey, A., Bai, J., De Gois, S., Delaby, E., Assouline, B., Guinchat, V., Devillard, F., Delorme, R., Nygren, G., Meier, J., Otani, S., Cheval, H., James, V., Topf, M., Dear, N., Gillberg, C., Leboyer, M., Giros, B., Gautron, S., Hazan, J., Harvey, R., Legendre, P. & Betancur, C. 2016 In : Molecular Psychiatry. 21, p. 936-945

    Research output: Contribution to journalArticle

  5. 2015
  6. Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.

    Renström, F. , Franks, P. & 152 others Cornelis, M. C., Byrne, E. M., Esko, T., Nalls, M. A., Ganna, A., Paynter, N., Monda, K. L., Amin, N., Fischer, K., Ngwa, J. S., Huikari, V., Cavadino, A., Nolte, I. M., Teumer, A., Yu, K., Marques-Vidal, P., Rawal, R., Manichaikul, A., Wojczynski, M. K., Vink, J. M., Zhao, J. H., Burlutsky, G., Lahti, J., Mikkilä, V., Lemaitre, R. N., Eriksson, J., Musani, S. K., Tanaka, T., Geller, F., Luan, J., Hui, J., Mägi, R., Dimitriou, M., Garcia, M. E., Ho, W-K., Wright, M. J., Rose, L. M., Magnusson, P. K. E., Pedersen, N. L., Couper, D., Oostra, B. A., Hofman, A., Ikram, M. A., Tiemeier, H. W., Uitterlinden, A. G., van Rooij, F. J. A., Barroso, I., Johansson, I., Xue, L., Kaakinen, M., Milani, L., Power, C., Snieder, H., Stolk, R. P., Baumeister, S. E., Biffar, R., Gu, F., Bastardot, F., Kutalik, Z., Jacobs, D. R., Forouhi, N. G., Mihailov, E., Lind, L., Lindgren, C., Michaëlsson, K., Morris, A., Jensen, M., Khaw, K-T., Luben, R. N., Wang, J. J., Männistö, S., Perälä, M-M., Kähönen, M., Lehtimäki, T., Viikari, J., Mozaffarian, D., Mukamal, K., Psaty, B. M., Döring, A., Heath, A. C., Montgomery, G. W., Dahmen, N., Carithers, T., Tucker, K. L., Ferrucci, L., Boyd, H. A., Melbye, M., Treur, J. L., Mellström, D., Hottenga, J. J., Prokopenko, I., Tönjes, A., Deloukas, P., Kanoni, S., Lorentzon, M., Houston, D. K., Liu, Y., Danesh, J., Rasheed, A., Mason, M. A., Zonderman, A. B., Franke, L., Kristal, B. S., Karjalainen, J., Reed, D. R., Westra, H-J., Evans, M. K., Saleheen, D., Harris, T. B., Dedoussis, G., Curhan, G., Stumvoll, M., Beilby, J., Pasquale, L. R., Feenstra, B., Bandinelli, S., Ordovas, J. M., Chan, A. T., Peters, U., Ohlsson, C., Gieger, C., Martin, N. G., Waldenberger, M., Siscovick, D. S., Raitakari, O., Eriksson, J. G., Mitchell, P., Hunter, D. J., Kraft, P., Rimm, E. B., Boomsma, D. I., Borecki, I. B., Loos, R. J. F., Wareham, N. J., Vollenweider, P., Caporaso, N., Grabe, H. J., Neuhouser, M. L., Wolffenbuttel, B. H. R., Hu, F. B., Hyppönen, E., Järvelin, M-R., Cupples, L. A., Ridker, P. M., van Duijn, C. M., Heiss, G., Metspalu, A., North, K. E., Ingelsson, E., Nettleton, J. A., van Dam, R. M. & Chasman, D. I. 2015 In : Molecular Psychiatry. 20, 5, p. 647-656

    Research output: Contribution to journalArticle

  7. 2014
  8. The KMO allele encoding Arg(452) is associated with psychotic features in bipolar disorder type 1, and with increased CSF KYNA level and reduced KMO expression

    Lavebratt, C., Olsson, S., Backlund, L., Frisen, L., Sellgren, C., Priebe, L., Nikamo, P., Lil Träskman Bendz, Cichon, S., Vawter, M. P., Osby, U., Engberg, G., Landen, M., Erhardt, S. & Schalling, M. 2014 In : Molecular Psychiatry. 19, 3, p. 334-341

    Research output: Contribution to journalArticle

  9. 2008
  10. Abnormal melatonin synthesis in autism spectrum disorders

    Råstam, M. & 21 others Melke, J., Goubran-Botros, H., Chaste, P., Betancur, C., Nygren, G., Anckarsäter, H., Ståhlberg, O., Gillberg, I. C., D3elorme, R., Chabane, N., Mouren-Simeoni, M-C., Fauchereau, F., Durand, C. M., Chevalier, F., Drouot, X., Collet, C., Launay, J-M., Leboyer, M., Gilblerg, C., Bourgeron, T. & and, T. P. S. 2008 In : Molecular Psychiatry. 13, 1, p. 90-98

    Research output: Contribution to journalArticle

  11. 2005
  12. Support for the association between the rare functional variant 1425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder

    Råstam, M. & 23 others Delorme, R., Betancur, C., Wagner, M., Krebs, M-O., Gorwood, P., Pearl, P., Nygren, G., Durand, C. M., Buhtz, F., Pickering, P., Melke, J., Ruhrmann, S., Anckarsäter, H., Chabane, N., Kipman, A., Reck, C., Millet, B., Roy, I., Mouren-Simeoni, M-C., Maier, W., Gillberg, C., Leboyer, M. & Bourgeron, T. 2005 In : Molecular Psychiatry. 10, 12, p. 1059-61

    Research output: Contribution to journalArticle